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Project Revoice
Project Revoice is a initiative with the ultimate goal to ensure that no one living with ALS will ever have to suffer being robbed of their voice.
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National ALS Registry
The National ALS Registry is a congressionally mandated registry for persons in the U.S. with ALS. It is the only population-based registry in the U.S. that collects information to help scientists learn more about who gets ALS and its causes.
Learn MoreWhether you’re newly diagnosed, navigating your journey with the disease, caring for a person with ALS, or researching the cure, there are resources to support you.
Let us help you and your family cope with the day-to-day challenges of living with ALS.
For People with ALS
Learn about our grant program, upcoming scientific meetings, and opportunities to collaborate.
For Researchers
Caring for someone with ALS is hard work. We offer resources and support to help you.
For Caregivers- The ALS Association Fights To Protect Health Care Access After Texas Ruling
December 17, 2018 - SOD1 Phase I Antisense Trial Shows Promise and C9orf72 Phase I Antisense Trial Begins
December 17, 2018 - Motor Neuron Excitability is Reduced in People with ALS Following Ezogabine Treatment
December 14, 2018 - Guest Post: ‘It Takes A Village’
December 12, 2018
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Your gift will help The ALS Association support research to find a cure for ALS and provide much-needed services to patients and their families. By becoming a part of The ALS Association family and making your gift today, you will help sustain hope in thousands of people affected by ALS.